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Suledine - HIV - Taiwan Registration 53f6731f4b58d092b7ac4bdfd0a4e673

Access comprehensive regulatory information for Suledine - HIV in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 53f6731f4b58d092b7ac4bdfd0a4e673 and manufactured by FUJIREBIO, Inc., Hachioji Facility. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical Co., Ltd.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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53f6731f4b58d092b7ac4bdfd0a4e673
Registration Details
Taiwan FDA Registration: 53f6731f4b58d092b7ac4bdfd0a4e673
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Device Details

Suledine - HIV
TW: ้€Ÿๆจ‚ๅฎš-HIV
Risk Class 3
Cancelled

Registration Details

53f6731f4b58d092b7ac4bdfd0a4e673

DHA00601228008

Company Information

Product Details

Particle agglutination test for human immunodeficiency virus antibodies (anti-HIV) for screening.

B Hematology, pathology, and genetics

import

Dates and Status

Sep 09, 2005

Aug 01, 2018

Jun 16, 2022

Cancellation Information

Logged out

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